Cargando…
Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion
Coxsackievirus A6 (CV-A6) has recently overtaken enterovirus A71 and CV-A16 as the primary causative agent of hand, foot, and mouth disease worldwide. Virions of CV-A6 were not identified in previous structural studies, and it was speculated that the virus is unique among enteroviruses in using alte...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438360/ https://www.ncbi.nlm.nih.gov/pubmed/36056184 http://dx.doi.org/10.1038/s42003-022-03863-2 |
_version_ | 1784781811692339200 |
---|---|
author | Büttner, Carina R. Spurný, Radovan Füzik, Tibor Plevka, Pavel |
author_facet | Büttner, Carina R. Spurný, Radovan Füzik, Tibor Plevka, Pavel |
author_sort | Büttner, Carina R. |
collection | PubMed |
description | Coxsackievirus A6 (CV-A6) has recently overtaken enterovirus A71 and CV-A16 as the primary causative agent of hand, foot, and mouth disease worldwide. Virions of CV-A6 were not identified in previous structural studies, and it was speculated that the virus is unique among enteroviruses in using altered particles with expanded capsids to infect cells. In contrast, the virions of other enteroviruses are required for infection. Here we used cryo-electron microscopy (cryo-EM) to determine the structures of the CV-A6 virion, altered particle, and empty capsid. We show that the CV-A6 virion has features characteristic of virions of other enteroviruses, including a compact capsid, VP4 attached to the inner capsid surface, and fatty acid-like molecules occupying the hydrophobic pockets in VP1 subunits. Furthermore, we found that in a purified sample of CV-A6, the ratio of infectious units to virions is 1 to 500. Therefore, it is likely that virions of CV-A6 initiate infection, like those of other enteroviruses. Our results provide evidence that future vaccines against CV-A6 should target its virions instead of the antigenically distinct altered particles. Furthermore, the structure of the virion provides the basis for the rational development of capsid-binding inhibitors that block the genome release of CV-A6. |
format | Online Article Text |
id | pubmed-9438360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94383602022-09-02 Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion Büttner, Carina R. Spurný, Radovan Füzik, Tibor Plevka, Pavel Commun Biol Article Coxsackievirus A6 (CV-A6) has recently overtaken enterovirus A71 and CV-A16 as the primary causative agent of hand, foot, and mouth disease worldwide. Virions of CV-A6 were not identified in previous structural studies, and it was speculated that the virus is unique among enteroviruses in using altered particles with expanded capsids to infect cells. In contrast, the virions of other enteroviruses are required for infection. Here we used cryo-electron microscopy (cryo-EM) to determine the structures of the CV-A6 virion, altered particle, and empty capsid. We show that the CV-A6 virion has features characteristic of virions of other enteroviruses, including a compact capsid, VP4 attached to the inner capsid surface, and fatty acid-like molecules occupying the hydrophobic pockets in VP1 subunits. Furthermore, we found that in a purified sample of CV-A6, the ratio of infectious units to virions is 1 to 500. Therefore, it is likely that virions of CV-A6 initiate infection, like those of other enteroviruses. Our results provide evidence that future vaccines against CV-A6 should target its virions instead of the antigenically distinct altered particles. Furthermore, the structure of the virion provides the basis for the rational development of capsid-binding inhibitors that block the genome release of CV-A6. Nature Publishing Group UK 2022-09-02 /pmc/articles/PMC9438360/ /pubmed/36056184 http://dx.doi.org/10.1038/s42003-022-03863-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Büttner, Carina R. Spurný, Radovan Füzik, Tibor Plevka, Pavel Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion |
title | Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion |
title_full | Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion |
title_fullStr | Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion |
title_full_unstemmed | Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion |
title_short | Cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus A6 virion |
title_sort | cryo-electron microscopy and image classification reveal the existence and structure of the coxsackievirus a6 virion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438360/ https://www.ncbi.nlm.nih.gov/pubmed/36056184 http://dx.doi.org/10.1038/s42003-022-03863-2 |
work_keys_str_mv | AT buttnercarinar cryoelectronmicroscopyandimageclassificationrevealtheexistenceandstructureofthecoxsackievirusa6virion AT spurnyradovan cryoelectronmicroscopyandimageclassificationrevealtheexistenceandstructureofthecoxsackievirusa6virion AT fuziktibor cryoelectronmicroscopyandimageclassificationrevealtheexistenceandstructureofthecoxsackievirusa6virion AT plevkapavel cryoelectronmicroscopyandimageclassificationrevealtheexistenceandstructureofthecoxsackievirusa6virion |